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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GALE
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign/Likely benign
GALE
(K257R)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity; other